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Genes Relevant to Tissue Response to Cancer Therapy Display Diurnal Variation in mRNA Expression in Human Oral Mucosa.
Gu, Fangyi; Gomez, Eduardo Cortes; Chen, Jianhong; Buas, Matthew F; Schlecht, Nicolas F; Hulme, Karen; Kulkarni, Shweta Vishwas; Singh, Prashant K; O'Connor, Richard; Ambrosone, Christine B; Singh, Anurag K; Wang, Jianmin.
Afiliação
  • Gu F; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, US.
  • Gomez EC; Department of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, US.
  • Chen J; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, US.
  • Buas MF; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, US.
  • Schlecht NF; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, US.
  • Hulme K; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, US.
  • Kulkarni SV; School of Public Health, University of Buffalo, US.
  • Singh PK; Center for Personalized Medicine, Roswell Park Comprehensive Cancer Center, US.
  • O'Connor R; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, US.
  • Ambrosone CB; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, US.
  • Singh AK; Department of Radiation Medicine, Roswell Park Comprehensive Cancer Center, US.
  • Wang J; Department of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, US.
J Circadian Rhythms ; 19: 8, 2021 Jun 17.
Article em En | MEDLINE | ID: mdl-34221066
ABSTRACT

BACKGROUND:

To address a critical gap for application of cancer chronotherapy of when would be the best time(s) for treating an individual cancer patient, we conducted a pilot study to characterize diurnal variations of gene expression in oral mucosal tissue, which is vulnerable to damage from cancer therapies.

METHODS:

We conducted RNA-seq assay on individual oral mucosal samples collected from 11 healthy volunteers every 4 hours (6 time points). Using a cosine-based method, we estimated the individual and average values of peak-time and amplitude for each gene. Correlations between gene expression peak-times and age was examined, adjusting for individual's sleep timing.

RESULTS:

Among candidate gene pathways that are relevant to treatment response, 7 of 16 genes (PER3, CIART, TEF, PER1, PER2, CRY2, ARNTL) involved in circadian regulation and 1 of 118 genes (WEE1) involved in cell cycle regulation achieved p-value ≤ 0.1 and relative amplitude>0.1. The average peak times were approximately 1015 for PER3, CIART and TEF, 1045 for PER1, 1300 for WEE1, PER2 and CRY2, and 1930 for ARNTL. Ranges in peak times across individuals differed by gene (e.g., 8 hours for PER1; 16.7 hours for WEE1). Older people had later peak times for PER1 (r = 0.77, p = 0.03) and PER3 (r = 0.69, p-value = 0.06).

CONCLUSION:

In oral mucosa, expression of some genes relevant to treatment response displayed diurnal variation. These genes may be candidates for development of biomarkers for optimizing individual timing of cancer therapy using non-invasively collected oral mucosa.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article